Drug recall
A mobile, electro-hydraulically operated, fluoroscopic/C-Arm compatible general surgical table. Product Usage…
FDA recall event 54705 · Class II · Steris Corporation
Key facts
| Event ID | 54705 |
|---|---|
| Recall numbers | Z-2402-2012 |
| Recalling firm | Steris Corporation |
| Product type | Devices |
| Products | A mobile, electro-hydraulically operated, fluoroscopic/C-Arm compatible general surgical table. Product Usage: Product provides a flexible, easy-to-use, articulated posturing of a patient for either… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Customers may be storing objects on the base and/or around the column of the surgical table. This prohibited practice and misuse known by the customers can damage the override switch assembly located… |
| Initiation date | Feb 17, 2010 |
| Report date | Sep 26, 2012 |
| Termination date | Mar 13, 2013 |
| City | Mentor |
| State | OH |
| Country | United States |
| FEI number | 1527821 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: